| Literature DB >> 11137106 |
K E Heath1, M Gahan, R A Whittall, S E Humphries.
Abstract
Mutations in the low density lipoprotein receptor gene (LDLR) cause familial hypercholesterolaemia (FH). The FH website (http://www.ucl. ac.uk/fh) has been updated to provide various functions enabling the analysis of the large number of LDLR mutations. To date, 683 LDLR mutations have been reported; of these 58.9% are missense mutations, 21.1% minor rearrangements, 13.5% major rearrangements and 6.6% splice site mutations. Of the 402 missense mutations, only 11.4% occurred at CpG sites. The majority of mutations were found in two functional domains, the ligand binding domain (42%) and the epidermal growth factor (EGF) precursor-like domain (47%). This report describes new features of the FH website and assesses the spectrum of mutations reported to date.Entities:
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Year: 2001 PMID: 11137106 DOI: 10.1016/s0021-9150(00)00647-x
Source DB: PubMed Journal: Atherosclerosis ISSN: 0021-9150 Impact factor: 5.162